HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 2-(2,3,5-Trichlorophenyl)-4-methoxy-3-oxo-butyronitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Ethyl 2-methoxyacetate | HCID 77544 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | 2-(2,3,5-Trichlorophenyl)acetonitrile | HCID 19705099 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | 2-(2,3,5-Trichlorophenyl)-4-methoxy-3-oxo-butyronitrile | HCID 19705085 | — |
Reaction Steps
To a stirred refluxing solution of sodium ethoxide (from 1.38 g sodium) in ethanol (25 ml) was added over 5 minutes a mixture of 2,3,5-trichlorophenylacetonitrile (11 g) and ethyl methoxyacetate (8.85 g) in dry DME (25 ml). After 4 hours the mixture was cooled on ice and acidified by dropwise addition of acetic acid (ca. 6 ml), diluted with ice-water (150 ml) and extracted with dichloromethane (2×100 ml). The dichloromethane extract was washed with water, dried over MgSO4 and concentrated giving a yellow solid, which was triturated with a little ether and filtered. 8.6 g Homogeneous by TLC (19:1 CH2Cl2 :MeOH).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05136080 |
| Source dataset | uspto-grants-1992_08 |
| ORD ID | ord-6d25ad1cfff242cea94330f60e356386 |
| Source note | uspto-grants-1992_08 |